Basic information Safety Supplier Related

2-dibenzofuranamine

Basic information Safety Supplier Related

2-dibenzofuranamine Basic information

Product Name:
2-dibenzofuranamine
Synonyms:
  • 2-ado
  • 2-aminodibenzofuran
  • 2-dibenzofuranamine
  • Dibenzofuran-2-amine
  • dibenzofuran-2-ylamine
  • 2-AMinodiphenylene Oxide
  • NSC 402280
  • dibenzo[b,d]furan-2-amine
CAS:
3693-22-9
MF:
C12H9NO
MW:
183.21
Mol File:
3693-22-9.mol
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2-dibenzofuranamine Chemical Properties

Melting point:
128°C
Boiling point:
316.88°C (rough estimate)
Density 
1.1261 (rough estimate)
refractive index 
1.5880 (estimate)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
powder to crystal
pka
3.91±0.30(Predicted)
color 
White to Orange to Green
Stability:
Stability
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Safety Information

HS Code 
2932.99.7000
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2-dibenzofuranamine Usage And Synthesis

Uses

2-Aminodibenzofuran is a polycyclic aromatic hydrocarbon (PAH) used in the preparation of mono and bisazo dyes. 2-Aminodibenzofuran is a carcinogen.

Synthesis Reference(s)

Tetrahedron Letters, 25, p. 429, 1984 DOI: 10.1016/S0040-4039(00)99903-9

Synthesis

86-76-0

3693-22-9

GENERAL METHOD: In a flame-dried reaction vial, 2-bromodibenzo[b,d]furan (1.0 mmol, 1.0 eq.) was dissolved in 2 mL of anhydrous THF. A hexane solution of n-butyllithium (1.1 mmol, 1.1 eq.) was slowly added at -78 °C and maintained at this temperature.After 30 min, this aryllithium solution was transferred to MgBr2 (1.0 mmol, 1.0 eq., reprepared from magnesium and 1,2-dibromoethane) previously suspended at -78 °C. The reaction mixture was allowed to warm naturally to room temperature over 30 min and subsequently cooled to the target temperature T. An anhydrous toluene solution (1.2 mL) of oxalidine (1.2 mmol, 1.2 eq.) was added to the reaction mixture at temperature T. The reaction was continued for a period of 30 min. The reaction was stirred continuously for 2 h at the target temperature T, after which the reaction was quenched with saturated aqueous NH4Cl solution. (The specific reaction temperature and time need to be adjusted according to the actual conditions of each substrate.)

References

[1] Patent: US2018/57444, 2018, A1. Location in patent: Paragraph 0098; 0142; 0143; 0222; 0257
[2] Journal of the American Chemical Society, 1934, vol. 56, p. 2473,2476
[3] Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 20, p. 436,437
[4] Tetrahedron Letters, 1984, vol. 25, # 4, p. 429 - 432
[5] Chemical & Pharmaceutical Bulletin, 1986, vol. 34, # 4, p. 1524 - 1530

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